The year-end FDA registration and listing cycle can create avoidable pressure when establishment and product listing information needs to be reviewed or updated. Join LexisNexis Life Sciences Solutions...
Your EUDAMED readiness checklist for actor, certificate, product, and UDI data The first four EUDAMED modules became mandatory on May 28, 2026, making EUDAMED an immediate operational requirement for...
Opus Regulatory — Washington, DC | October 20 We'll be at Opus Regulatory's Global Labeling and Regulatory Symposium in Washington, DC. Come find our team to discuss how LexisNexis supports...
Regulatory Affairs Professionals Society — Charlotte, North Carolina | September 15–17 Meet us at RAPS Convergence 2026 in Charlotte — the flagship event for regulatory affairs professionals...
Informa Connect — Berlin, Germany | June 15–18 Find us at the MedTech Summit in Berlin, where regulatory affairs professionals and industry leaders tackle MDR/IVDR compliance and market access...
The year-end FDA registration and listing cycle can create avoidable pressure when establishment and product listing information needs to be reviewed or updated. Join LexisNexis Life Sciences Solutions regulatory experts for an interactive discussion on preparing for annual registration renewals, listing certifications, and related updates before the deadline.
This interview-style session will feature questions submitted by attendees, along with insights based on common issues our experts encounter while supporting pharmaceutical companies.
Mary Frasch LexisNexis Life Sciences Solutions, Senior Regulatory Consultant
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Dennis Lingg LexisNexis Life Sciences, Regulatory Consultant
Rachel Finley LexisNexis Life Sciences, Senior Regulatory Consultant
Dan Clark LexisNexis Life Sciences, Technical Consultant
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